-
1
-
-
0024446959
-
Food iron absorption in idiopathic hemochromatosis
-
Lynch SR, Skikne BS, Cook JD. Food iron absorption in idiopathic hemochromatosis. Blood 1989;74:2187-93.
-
(1989)
Blood
, vol.74
, pp. 2187-2193
-
-
Lynch, S.R.1
Skikne, B.S.2
Cook, J.D.3
-
2
-
-
0025824547
-
Regulation of intestinal iron absorption and mucosal iron kinetics in hereditary hemochromatosis
-
McLaren GD, Nathanson MH, Jacobs A, Trevett D, Thomson W. Regulation of intestinal iron absorption and mucosal iron kinetics in hereditary hemochromatosis. J Lab Clin Med 1991;117:390-401.
-
(1991)
J Lab Clin Med
, vol.117
, pp. 390-401
-
-
McLaren, G.D.1
Nathanson, M.H.2
Jacobs, A.3
Trevett, D.4
Thomson, W.5
-
3
-
-
84965275514
-
Iron absorption in idiopathic haemochromatosis before, during, and after venesection therapy
-
Williams R, Manenti F, Williams HS, Pitcher CS. Iron absorption in idiopathic haemochromatosis before, during, and after venesection therapy. BMJ 1966;2:78-81.
-
(1966)
BMJ
, vol.2
, pp. 78-81
-
-
Williams, R.1
Manenti, F.2
Williams, H.S.3
Pitcher, C.S.4
-
4
-
-
0034863686
-
Genetic hemochromatosis, a Celtic disease: Is it now time for population screening?
-
Byrnes V, Ryan E, Barrett S, Kenny P, Mayne P, Crowe J. Genetic hemochromatosis, a Celtic disease: is it now time for population screening? Genet Testing 2001;5:127-30.
-
(2001)
Genet Testing
, vol.5
, pp. 127-130
-
-
Byrnes, V.1
Ryan, E.2
Barrett, S.3
Kenny, P.4
Mayne, P.5
Crowe, J.6
-
5
-
-
0141455095
-
A method for detecting recent selection in the human genome from allele age estimates
-
Toomajian C, Ajioka RS, Jorde LB, Kushner JP, Kreitman M. A method for detecting recent selection in the human genome from allele age estimates. Genetics 2003;165:287-97.
-
(2003)
Genetics
, vol.165
, pp. 287-297
-
-
Toomajian, C.1
Ajioka, R.S.2
Jorde, L.B.3
Kushner, J.P.4
Kreitman, M.5
-
6
-
-
18344401294
-
Multicentric origin of hemochromatosis gene (HFE) mutations
-
Rochette J, Pointon JJ, Fisher CA, et al. Multicentric origin of hemochromatosis gene (HFE) mutations. Am J Hum Genet 1999;64:1056-62.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1056-1062
-
-
Rochette, J.1
Pointon, J.J.2
Fisher, C.A.3
-
7
-
-
5144232051
-
Iron absorption by heterozygous carriers of the HFE C282Y mutation associated with hemochromatosis
-
Hunt JR, Zeng H. Iron absorption by heterozygous carriers of the HFE C282Y mutation associated with hemochromatosis. Am J Clin Nutr 2004;80:924-31.
-
(2004)
Am J Clin Nutr
, vol.80
, pp. 924-931
-
-
Hunt, J.R.1
Zeng, H.2
-
8
-
-
0031700041
-
Heterozygosity for the C282Y mutation in the hemochromatosis gene is associated with increased serum iron, transferrin saturation, and hemoglobin in young women: A protective role against iron deficiency?
-
Datz C, Haas T, Rinner H, Sandhofer F, Patsch W, Paulweber B. Heterozygosity for the C282Y mutation in the hemochromatosis gene is associated with increased serum iron, transferrin saturation, and hemoglobin in young women: a protective role against iron deficiency? Clin Chem 1998;44:2429-32.
-
(1998)
Clin Chem
, vol.44
, pp. 2429-2432
-
-
Datz, C.1
Haas, T.2
Rinner, H.3
Sandhofer, F.4
Patsch, W.5
Paulweber, B.6
-
9
-
-
0344837836
-
Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry
-
Beutler E, Felitti V, Gelbart T, Waalen J. Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry. Br J Haematol 2003;120:887-93.
-
(2003)
Br J Haematol
, vol.120
, pp. 887-893
-
-
Beutler, E.1
Felitti, V.2
Gelbart, T.3
Waalen, J.4
-
10
-
-
1642566560
-
Hemochromatosis and the enigma of misplaced iron: Implications for infectious disease and survival
-
Moalem S, Weinberg ED, Percy ME. Hemochromatosis and the enigma of misplaced iron: implications for infectious disease and survival. Biometals 2004;17:135-9.
-
(2004)
Biometals
, vol.17
, pp. 135-139
-
-
Moalem, S.1
Weinberg, E.D.2
Percy, M.E.3
-
11
-
-
0038542813
-
The HFE Cys282Tyr mutation as a necessary but not sufficient cause of hereditary hemochromatosis
-
Beutler E. The HFE Cys282Tyr mutation as a necessary but not sufficient cause of hereditary hemochromatosis. Blood 2003;101:3347-50.
-
(2003)
Blood
, vol.101
, pp. 3347-3350
-
-
Beutler, E.1
|